19
views
0
recommends
+1 Recommend
1 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network’s first protocol: deep phenotyping in three sub-Saharan African countries

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network is a new and broadly-based group of research scientists and health advocates based in the UK, Africa and North America.

          Methods

          This paper describes the protocol that underpins the clinical research activity of the Network, so that the investigators, and broader global health community, can have access to ‘deep phenotyping’ (social determinants of health, demographic and clinical parameters, placental biology and agnostic discovery biology) of women as they advance through pregnancy to the end of the puerperium, whether those pregnancies have normal outcomes or are complicated by one/more of the placental disorders of pregnancy (pregnancy hypertension, fetal growth restriction and stillbirth). Our clinical sites are in The Gambia (Farafenni), Kenya (Kilifi County), and Mozambique (Maputo Province). In each country, 50 non-pregnant women of reproductive age will be recruited each month for 1 year, to provide a final national sample size of 600; these women will provide culturally-, ethnically-, seasonally- and spatially-relevant control data with which to compare women with normal and complicated pregnancies. Between the three countries we will recruit ≈10,000 unselected pregnant women over 2 years. An estimated 1500 women will experience one/more placental complications over the same epoch. Importantly, as we will have accurate gestational age dating using the TraCer device, we will be able to discriminate between fetal growth restriction and preterm birth. Recruitment and follow-up will be primarily facility-based and will include women booking for antenatal care, subsequent visits in the third trimester, at time-of-disease, when relevant, during/immediately after birth and 6 weeks after birth.

          Conclusions

          To accelerate progress towards the women’s and children’s health-relevant Sustainable Development Goals, we need to understand how a variety of social, chronic disease, biomarker and pregnancy-specific determinants health interact to result in either a resilient or a compromised pregnancy for either mother or fetus/newborn, or both. This protocol has been designed to create such a depth of understanding. We are seeking funding to maintain the cohort to better understand the implications of pregnancy complications for both maternal and child health.

          Related collections

          Most cited references32

          • Record: found
          • Abstract: found
          • Article: not found

          Prediction of adverse maternal outcomes in pre-eclampsia: development and validation of the fullPIERS model.

          Pre-eclampsia is a leading cause of maternal deaths. These deaths mainly result from eclampsia, uncontrolled hypertension, or systemic inflammation. We developed and validated the fullPIERS model with the aim of identifying the risk of fatal or life-threatening complications in women with pre-eclampsia within 48 h of hospital admission for the disorder. We developed and internally validated the fullPIERS model in a prospective, multicentre study in women who were admitted to tertiary obstetric centres with pre-eclampsia or who developed pre-eclampsia after admission. The outcome of interest was maternal mortality or other serious complications of pre-eclampsia. Routinely reported and informative variables were included in a stepwise backward elimination regression model to predict the adverse maternal outcome. We assessed performance using the area under the curve (AUC) of the receiver operating characteristic (ROC). Standard bootstrapping techniques were used to assess potential overfitting. 261 of 2023 women with pre-eclampsia had adverse outcomes at any time after hospital admission (106 [5%] within 48 h of admission). Predictors of adverse maternal outcome included gestational age, chest pain or dyspnoea, oxygen saturation, platelet count, and creatinine and aspartate transaminase concentrations. The fullPIERS model predicted adverse maternal outcomes within 48 h of study eligibility (AUC ROC 0·88, 95% CI 0·84-0·92). There was no significant overfitting. fullPIERS performed well (AUC ROC >0·7) up to 7 days after eligibility. The fullPIERS model identifies women at increased risk of adverse outcomes up to 7 days before complications arise and can thereby modify direct patient care (eg, timing of delivery, place of care), improve the design of clinical trials, and inform biomedical investigations related to pre-eclampsia. Canadian Institutes of Health Research; UNDP/UNFPA/WHO/World Bank Special Programme of Research, Development, and Research Training in Human Reproduction; Preeclampsia Foundation; International Federation of Obstetricians and Gynecologists; Michael Smith Foundation for Health Research; and Child and Family Research Institute. Copyright © 2011 Elsevier Ltd. All rights reserved.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            Preventing deaths due to the hypertensive disorders of pregnancy

            In this chapter, taking a life cycle and both civil society and medically oriented approach, we will discuss the contribution of the hypertensive disorders of pregnancy (HDPs) to maternal, perinatal and newborn mortality and morbidity. Here we review various interventions and approaches to preventing deaths due to HDPs and discuss effectiveness, resource needs and long-term sustainability of the different approaches. Societal approaches, addressing sustainable development goals (SDGs) 2.2 (malnutrition), 3.7 (access to sexual and reproductive care), 3.8 (universal health coverage) and 3c (health workforce strengthening), are required to achieve SDGs 3.1 (maternal survival), 3.2 (perinatal survival) and 3.4 (reduced impact of non-communicable diseases (NCDs)). Medical solutions require greater clarity around the classification of the HDPs, increased frequency of effective antenatal visits, mandatory responses to the HDPs when encountered, prompt provision of life-saving interventions and sustained surveillance for NCD risk for women with a history of the HDPs.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Shock index: an effective predictor of outcome in postpartum haemorrhage?

              To compare the predictive value of the shock index (SI) with conventional vital signs in postpartum haemorrhage (PPH), and to establish 'alert' thresholds for use in low-resource settings.
                Bookmark

                Author and article information

                Contributors
                pvd@kcl.ac.uk
                Journal
                Reprod Health
                Reprod Health
                Reproductive Health
                BioMed Central (London )
                1742-4755
                30 April 2020
                30 April 2020
                2020
                : 17
                Issue : Suppl 1 Issue sponsor : The PRECISE Network: Deep phenotyping of pregnancies in Africa
                : 51
                Affiliations
                [1 ]ISNI 0000 0001 2322 6764, GRID grid.13097.3c, Department of Women and Children’s Health, School of Life Course Science, Faculty of Life Sciences and Medicine, , King’s College London, ; 5th Floor, Becket House, 1 Lambeth Palace Road, London, SE1 7EU UK
                [2 ]ISNI 0000 0004 1936 8948, GRID grid.4991.5, Nuffield Department of Women’s and Reproductive Health, , University of Oxford, ; Oxford, UK
                [3 ]Donna Russell Consulting, Seattle, WA USA
                [4 ]ISNI 0000 0004 0606 294X, GRID grid.415063.5, Medical Research Council Unit (The Gambia) at the London School of Hygiene and Tropical Medicine, ; Fajara, The Gambia
                [5 ]GRID grid.470490.e, Centre of Excellence in Women and Child Health, East Africa, , Aga Khan University in East Africa, ; Nairobi, Kenya
                [6 ]ISNI 0000 0000 9638 9567, GRID grid.452366.0, Centro de Investigação em Saúde de Manhiça, ; Manhiça, Maputo Province, Mozambique
                [7 ]GRID grid.8295.6, Department of Physiological Science, Clinical - Pharmacology, Faculty of Medicine, , Universidade Eduardo Mondlane, ; Maputo, Mozambique
                [8 ]ISNI 0000 0004 0425 469X, GRID grid.8991.9, MARCH Centre, , London School of Hygiene and Tropical Medicine, ; London, UK
                [9 ]ISNI 0000 0001 2322 6764, GRID grid.13097.3c, Department of Health Service and Population Research, Institute of Psychiatry, , King’s College London, ; London, UK
                [10 ]ISNI 0000 0001 2322 6764, GRID grid.13097.3c, Lau China Institute, Faculty of Social Science and Public Policy, , King’s College London, ; London, UK
                [11 ]ISNI 0000 0000 9894 9740, GRID grid.442709.c, Department of Surveying and Geomatics, , Midlands State University, ; Gweru, Zimbabwe
                Article
                872
                10.1186/s12978-020-0872-9
                7191688
                32354357
                eb9c7cfd-0c1b-43e9-b138-ddbc4b5eb02e
                © The Author(s). 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                Categories
                Study Protocol
                Custom metadata
                © The Author(s) 2020

                Obstetrics & Gynecology
                pregnancy,africa south of the sahara,biorepository,pre-eclampsia,biological specimens

                Comments

                Comment on this article

                scite_
                0
                0
                0
                0
                Smart Citations
                0
                0
                0
                0
                Citing PublicationsSupportingMentioningContrasting
                View Citations

                See how this article has been cited at scite.ai

                scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.

                Similar content12

                Cited by11

                Most referenced authors490